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肌肉量低与克罗恩病生物制剂的疗效相关。

Low muscle mass is associated with efficacy of biologics in Crohn's disease.

机构信息

Department of Gastroenterology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.

Department of Neurology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.

出版信息

Clin Nutr. 2024 Oct;43(10):2354-2363. doi: 10.1016/j.clnu.2024.09.003. Epub 2024 Sep 5.

Abstract

BACKGROUND

Low muscle mass (LMM) can be a frequent complication in Crohn's disease (CD). We attempted to explore the effect of LMM on the efficacy of biologics in patients with CD.

METHODS

The retrospective cohort study included moderate-to-severe CD patients treated with infliximab or ustekinumab, and appendicitis patients as control. The skeletal muscle area (SMA) of L3 was assessed to evaluate the patients' muscle mass. After propensity score matching, the impact of LMM on drug efficacy was assessed in CD patients.

RESULTS

A total of 269 patients with CD and 172 appendicitis patients were included. The CD group had lower skeletal muscle density and BMI, and a higher risk of developing LMM than the control group. BMI (OR = 0.48, p < 0.001) and previous use of biologics (OR = 2.94, p = 0.019) were found to be independently associated with LMM. LMM was found to be associated with a decrease in clinical response (at weeks 8-14), clinical remission (at weeks 8-14, 24-30 and 52) and biochemical remission (at week 52). At weeks 24-30 and 52, LMM was independently associated with loss of response (LOR). We found LMM could be a predictor of lower clinical remission at week 30, lower clinical remission at week 52 and a higher LOR rate at week 30 in infliximab. While in ustekinumab, LMM was associated with lower endoscopic remission at week 24, biochemical remission at week 52 and a higher LOR rate at weeks 24 and 52.

CONCLUSIONS

The prevalence of LMM was higher in the CD group compared to the control group. For CD patients with LMM, the efficacy of infliximab and ustekinumab was relatively poor in both the short-term and long-term.

摘要

背景

低肌肉量(LMM)可能是克罗恩病(CD)的常见并发症。我们试图探讨 LMM 对 CD 患者生物制剂疗效的影响。

方法

本回顾性队列研究纳入了接受英夫利昔单抗或乌司奴单抗治疗的中重度 CD 患者,并以阑尾炎患者作为对照。评估 L3 的骨骼肌面积(SMA)以评估患者的肌肉量。在进行倾向评分匹配后,评估 LMM 对 CD 患者药物疗效的影响。

结果

共纳入 269 例 CD 患者和 172 例阑尾炎患者。与对照组相比,CD 组的骨骼肌密度和 BMI 较低,发生 LMM 的风险更高。BMI(OR=0.48,p<0.001)和既往使用生物制剂(OR=2.94,p=0.019)被发现与 LMM 独立相关。LMM 与临床应答(第 8-14 周)、临床缓解(第 8-14、24-30 和 52 周)和生化缓解(第 52 周)降低相关。在第 24-30 和 52 周时,LMM 与应答丧失(LOR)独立相关。我们发现 LMM 可以预测英夫利昔单抗第 30 周时临床缓解率较低,第 52 周时临床缓解率较低,第 30 周时 LOR 率较高。而在乌司奴单抗中,LMM 与第 24 周时内镜缓解率较低、第 52 周时生化缓解率较低以及第 24 和 52 周时 LOR 率较高相关。

结论

与对照组相比,CD 组的 LMM 患病率更高。对于 LMM 的 CD 患者,英夫利昔单抗和乌司奴单抗的短期和长期疗效均较差。

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